Job Title: Quality Control Analyst I

Location: Ridgefield, NJ

About the Job

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.

The Micro QC Analyst I is dedicated to the Microbiology Laboratory and EM Monitoring Program. The role of the Micro QC Analyst I will be that of various Microbial testing, EM monitoring of the aseptic production areas, ordering and stocking supplies, creating/reviewing SOPs, investigation writing, data entry.

• The candidate must have previous quality control microbiology experience. Experience in bioburden testing, membrane filtration, sterility isolator testing, conductivity, total organic carbon or endotoxin assays is preferred
  
• Basic knowledge of aseptic manufacturing environmental monitoring of Grade A-D Areas.
  
• SOP review, creation and approval is preferred
  
• OOS investigations writing is preferred
  
• Basic knowledge of compliance with all cGMP standards, safety and environmental regulations and company SOPs.
  
• Data entry of EM sampling results, LIMS, logbooks, and other miscellaneous lab data.
  
• Interact with Project Teams and cross-functional groups related to site operations
  
• Cohesive Micro player in the Micro department who is willing to assist or help a fellow analyst.
  

• Act for Change: Embrace change and innovation and initiate new and improved ways of working.
  
• Cooperate transversally: Collaborate effectively with peers, stakeholders and partners across the organization to positively impact business results.
  
• Develop People: Take responsibility for developing one's self and mentor other Micro Personnel in anticipation of future business needs or to assist the micro department.
  

• It is required that individuals care for their own safety and wellbeing. Individuals must promote a safe working environment for employees and contractors working in their area of responsibility.
  
• The individual must support all Sanofi and site HSE policies as well as ensure that work performed is compliant with local HSE regulations.
  
• Individuals must complete all required HSE trainings. Everyone is required to report all accidents and incidents and support investigations in their areas of responsibility. Individuals must ensure timely closure of HSE actions owned by their departments.
  

• BA/BS in Microbiology/Biology with at least 1 year of experience in CGMP, pharma or lab environment is required.
  
• Practical experience in general microbiology laboratory techniques working with bacteria, yeast and mold.
  
• Prior experience with data review, authoring SOPS, Change Controls, out of specification investigations and report writing is recommended.
  
• Working knowledge of cGMPs in pharmaceuticals/biological/aseptic/medical device manufacturing
  
• Excellent technical writing skills
  
• Ability to collaborate effectively with personnel and between departments
  
• Problem-solving skills
  
• Strong communicator
  
• Works independently
  
• Working knowledge of Word, Excel and PowerPoint
  

• Monday - Friday from 7:00 am to 3:30 pm, or Monday - Friday form 10:00 am to 6:30 pm
  
• Some flex in the start and end times may be allowed; weekend work and overtime as required.
  

• Bring the miracles of science to life alongside a supportive, future-focused team.
  
• Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
  
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.